Fluconazole Prophylaxis in Children with Acute Leukemia during Induction Chemotherapy in a Tertiary Care Hospital in Bangladesh.

Mymensingh medical journal : MMJ Pub Date : 2025-07-01
F Islam, S D M Taimur, T Sultana, I Nigar, A T M Rahman, C Y Jamal
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Abstract

Patients with hematological malignancies often develop febrile neutropenia (FN) as a complication of cancer chemotherapy. Opportunistic infection, especially invasive fungal infection (IFI) is frequently encountered during the neutropenic phase. With this perspective different anti-fungal agents had been tried as prophylaxis in leukemia. Evaluation of the role of fluconazole was as antifungal prophylaxis in children with acute leukemia during induction chemotherapy. This randomized double-blind placebo controlled prospective study was carried out in the Department of Pediatric Hematology and Oncology, Bangladesh Medical University (BMU), Bangladesh from September 2016 to August 2017. Total 60 (30 were in fluconazole and 30 were in placebo group) patients of age range from 1 to 18 years were included in this study. Mean age of the patients were 7.08±3.33 years in fluconazole group 6.29±2.79 years in placebo group. Male: Female ratio was 1.14:1. Out of total 60 patients 44 were ALL and 16 AML. Mean duration of neutropenia in fluconazole and placebo group were 13.40±5.75 days and placebo 16.83±5.77 days respectively. Success rate of fluconazole prophylaxis was 25(83.3%). Failure rates of placebo were 40.0%. Duration of empirical antifungal therapy in fluconazole and placebo group differed significantly (p=0.008). Difference of neutrophil recovery achievement in two groups was also significant (p=0.015). The mean duration from AFP to EAF therapy is 17.60±1.51 days and 14.33±5.72 days in patient with fluconazole and placebo group respectively. Prophylactic fluconazole can be used to decrease the fungal infection as well as the duration of febrile neutropenia during induction chemotherapy of Acute Leukemia in children.

氟康唑预防急性白血病儿童在诱导化疗期间在孟加拉国三级护理医院。
恶性血液病患者常出现发热性中性粒细胞减少症(FN)作为癌症化疗的并发症。机会性感染,特别是侵袭性真菌感染(IFI)在中性粒细胞减少期经常遇到。从这个角度来看,不同的抗真菌药物已被尝试作为白血病的预防。评价氟康唑在急性白血病患儿诱导化疗期间的抗真菌预防作用。这项随机双盲安慰剂对照前瞻性研究于2016年9月至2017年8月在孟加拉国医科大学(BMU)儿科血液学和肿瘤科进行。本研究共纳入60例患者(氟康唑组30例,安慰剂组30例),年龄1 ~ 18岁。氟康唑组平均年龄为7.08±3.33岁,安慰剂组平均年龄为6.29±2.79岁。男女比例为1.14:1。在总共60例患者中,44例为ALL, 16例为AML。氟康唑组和安慰剂组中性粒细胞减少的平均持续时间分别为13.40±5.75 d和16.83±5.77 d。氟康唑预防成功率25例(83.3%)。安慰剂组的失败率为40.0%。氟康唑组与安慰剂组经验抗真菌治疗时间差异有统计学意义(p=0.008)。两组中性粒细胞恢复率差异也有统计学意义(p=0.015)。氟康唑组和安慰剂组从AFP到EAF治疗的平均时间分别为17.60±1.51天和14.33±5.72天。儿童急性白血病诱导化疗期间预防性应用氟康唑可减少真菌感染,缩短发热性中性粒细胞减少的持续时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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